New highly cytotoxic organic and organometallic bexarotene derivatives

A series of bifunctional ruthenium(II) arene compounds modified with bexarotene, a retinoid that selectively activates retinoid X receptors inducing cell differentiation and apoptosis and preventing drug resistance, are described. The bexarotene is tethered to the ruthenium(II) arene fragment via an imidazole linker. Both the bexarotene-imidazole ligand and ruthenium(II) arene complexes are considerably more cytotoxic than the parent drug bexarotene. Docking studies show that the interactions of these compounds with possible targets are significantly different to the binding mode of the parent drug. (C) 2017 Elsevier B.V. All rights reserved.


Published in:
Journal Of Organometallic Chemistry, 839, 91-97
Year:
2017
Publisher:
Lausanne, Elsevier
ISSN:
0022-328X
Keywords:
Laboratories:




 Record created 2017-07-10, last modified 2018-01-28


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